Canonical Allele Identifier: CA1522556576

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1293994A= , CM000667.2:g.1293994A=	GRCh38
NC_000005.9:g.1294109A= , CM000667.1:g.1294109A=	GRCh37
NC_000005.8:g.1347109A=	NCBI36
NG_009265.1:g.6054T= , LRG_343:g.6054T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.892T= MANE Select	ENSP00000309572.5:p.Ser298=
ENST00000656021.1:c.892T=	ENSP00000499759.1:p.Ser298=
ENST00000310581.9:c.892T=	ENSP00000309572.5:p.Ser298=
ENST00000334602.10:c.892T=	ENSP00000334346.6:p.Ser298=
ENST00000460137.6:c.892T=	ENSP00000425003.1:p.Ser298=
ENST00000508104.2:c.892T=	ENSP00000426042.2:p.Ser298=
NM_001193376.1:c.892T=	NP_001180305.1:p.Ser298=
NM_198253.2:c.892T= , LRG_343t1:c.892T=	NP_937983.2:p.Ser298=
NR_149162.1:n.950T=
NR_149163.1:n.950T=
NM_001193376.2:c.892T=	NP_001180305.1:p.Ser298=
NM_198253.3:c.892T= MANE Select	NP_937983.2:p.Ser298=
NR_149162.2:n.971T=
NR_149163.2:n.971T=
NM_001193376.3:c.892T=	NP_001180305.1:p.Ser298=
NR_149162.3:n.971T=
NR_149163.3:n.971T=